Not so benign: Life-threatening hematuria from renal papillary necrosis in sickle cell trait

Renal papillary necrosis (RPN) is an uncommon but important cause of hematuria in patients with sickle cell trait. We report a 28-year-old female with sickle cell trait and beta thalassemia who developed recurrent, transfusion-dependent gross hematuria. Despite extensive imaging, endoscopic evaluati...

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Hlavní autoři:	Katharine Hodgen, Parth Joshi, Megan Ngai, Jeffrey Schiff
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Elsevier 2026-07-01
Edice:	Urology Case Reports
Témata:	Renal papillary necrosis Sickle cell trait Gross hematuria Aminocaproic acid Antifibrinolytic therapy Beta thalassemia
On-line přístup:	http://www.sciencedirect.com/science/article/pii/S2214442026001622
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